A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10006n54



Internal ID22777901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:112603041..112608776hg38UCSC Ensembl
chr5:111938738..111944473hg19UCSC Ensembl
chr5:111966637..111972372hg18UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg385736
hg195736
hg185736
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv599373, nsv599378, nsv599381, nsv599380, nsv599379
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10006n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss82
Observed Complex0
Frequencyn/a


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